Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-2772-2015 — Aliquot Delivery Kit (Syringe and Plunger); for use in open and percutaneous procedures to facilitate placement of bone cement in weakened or diminished bone

U.S. FDA — Device Enforcement · United States · 2015-08-20 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2772-2015
Date of alert
2015-08-20
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Orthovita, Inc., dBA Stryker Orthobiologics.
Product category
device
Product type
Devices
Reported risk: Two isolated instances of holes in the outer header bag component of the double barrier sterile packaging configuration
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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